Your browser doesn't support javascript.
loading
Clinical trials and evaluation of Chinese patent medicine for chronic obstructive pulmonary disease / 中国中药杂志
China Journal of Chinese Materia Medica ; (24): 2351-2357, 2022.
Artigo em Chinês | WPRIM | ID: wpr-928115
ABSTRACT
The clinical randomized controlled trials(RCTs) of Chinese patent medicine in the treatment of chronic obstructive pulmonary disease(COPD) were reviewed and analyzed to provide references for clinical research, guideline development, policy formulation, and quality improvement of clinical evidence. On the basis of the collection in the Traditional Chinese Medicine(TCM) Clinical Evidence Database System(EVDS), CNKI, Wanfang, SinoMed, Cochrane Library, PubMed, EMbase were searched for RCTs of Chinese patent medicine for COPD as a source of clinical evidence from database inception to December 31, 2019. The publication time, sample size, intervention and control measures, course of treatment, outcome indicators, and methodological quality of the trials were analyzed and evaluated. A total of 733 RCTs of Chinese patent medicine for COPD were included, among which 228 RCTs had a sample size higher than 100, accounting for 31.1% of total RCTs. Eighty-eight Chinese patent medicines were involved, including 40 oral medicines and 48 injections. A total of 327 RCTs mentioned intervention and control measures(Chinese patent medicine + conventional treatment vs conventional treatment), accounting for 43.0%. In addition, 94.40% of the RCTs reported the course of treatment, and 53.20% of the RCTs determined 8-14 d as the intervention course. The evaluation indicators adopted were numerous, among which physicochemical indicators(70.57%) and symptoms/signs(24.35%) were the most frequently employed. The operation of allocation concealment and blinding was not standard. Registration and the procedure related to ethics were mostly missing. The results indicate that there are prominent methodological problems in the clinical trials of Chinese patent medicine in the treatment of COPD, affecting the reliability and practicability of the trials. It is necessary to further standardize the design, implementation, and quality control of clinical trials of Chinese patent medicine in the treatment of COPD, highlight the clinical value of Chinese patent medicine for COPD, and improve the quality of evidence.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Medicamentos de Ervas Chinesas / China / Reprodutibilidade dos Testes / Ensaios Clínicos como Assunto / Doença Pulmonar Obstrutiva Crônica / Medicamentos sem Prescrição / Medicina Tradicional Chinesa Tipo de estudo: Ensaio Clínico Controlado / Estudo diagnóstico / Guia de Prática Clínica Limite: Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: China Journal of Chinese Materia Medica Ano de publicação: 2022 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Medicamentos de Ervas Chinesas / China / Reprodutibilidade dos Testes / Ensaios Clínicos como Assunto / Doença Pulmonar Obstrutiva Crônica / Medicamentos sem Prescrição / Medicina Tradicional Chinesa Tipo de estudo: Ensaio Clínico Controlado / Estudo diagnóstico / Guia de Prática Clínica Limite: Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: China Journal of Chinese Materia Medica Ano de publicação: 2022 Tipo de documento: Artigo